CRA Monitor - Pediatric Oncology M/F (M/F)

TempoPHARMA is looking for a Clinical Research Associate Monitor M/F to intervene in all operational activities related to the smooth running of clinical trials, from their preparation to their closure.

Your missions

• Participate in the validation of protocols, notably through a review of their operational consistency;
• Conduct selection and feasibility surveys with investigator centers;
• Participate in the CRF validation process;
• Participate in the logistical management of the product: simulations, choice of provider, and definition of the pharmacy circuit;
• Develop procedures specific to the trial, notably for imaging logistics and sampling;
• Write the Monitoring Plan;
• Develop implementation supports and slides;
• Conduct site initiation, monitoring, and close-out visits, on-site or remotely, and write the associated reports;
• Ensure the operational follow-up of studies: updating tracking tables, newsletters, and conducting translational research;
• Ensure document management: investigator site file and TMF;
• Organize co-steering meetings and teleconferences necessary for study follow-up;
• Develop and update documents required within the framework of amendments;
• Participate in the monitoring of center invoicing.

• Scientific training (Pharmacist, Physician, Master 2 in life sciences or equivalent)
• At least 2 years of experience in clinical trial monitoring in oncology
• Experience in pediatric oncology is particularly appreciated for this mission
• Autonomy, rigor, and excellent interpersonal skills
• Professional English required
• National mobility to be expected

Additional information

• Internal training center
• Tickets Restaurant card
• Family company health insurance
• Holiday bonuses
• Christmas gift vouchers
• Personalized integration and follow-up for the consultant